HRID1745332

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID21937291

2',6'-Dimethyl[1,1'-biphenyl]-4-carboxylic acid

C15H14O2

HCID30069035

未命名化合物

结构：CON=C1C[C@@H](C(=O)O)N(C(=O)OC(C)(C)C)C1

HCID58714586

未命名化合物

PRODUCTS

生成物

结构：CON=C1C[C@@H](C(=O)N[C@@H]2CCCC[C@@H]2C(N)=O)N(C(=O)c2ccc(-c3c(C)cccc3C)cc2)C1

HCID131725660

未命名化合物

PROCEDURE

实验过程

Following the general method as outlined in Example 22, starting from (2S,4EZ)-1-(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acid, 2′,6′-dimethyl[1,1′-biphenyl]-4-carboxylic acid, and (1S,2R)-2-aminocyclohexanecarboxamide, the title compound was obtained in 92% purity by HPLC. MS(ESI+): m/z=491.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-a256dcf7689e439a939b76309529bbb6
来源数据集: uspto-grants-2006_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07018988B2
来源说明: uspto-grants-2006_03

反应 SMILES

C(O[C:6]([N:8]1[CH2:12][C:11](=[N:13][O:14][CH3:15])[CH2:10][C@H:9]1[C:16]([OH:18])=O)=[O:7])(C)(C)C.[CH3:19][C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([CH3:26])[C:21]=1[C:27]1[CH:32]=[CH:31][C:30](C(O)=O)=[CH:29][CH:28]=1.[NH2:36][C@@H:37]1[CH2:42][CH2:41][CH2:40][CH2:39][C@@H:38]1[C:43]([NH2:45])=[O:44]>>[NH2:45][C:43]([C@H:38]1[CH2:39][CH2:40][CH2:41][CH2:42][C@H:37]1[NH:36][C:16]([C@@H:9]1[CH2:10][C:11](=[N:13][O:14][CH3:15])[CH2:12][N:8]1[C:6]([C:30]1[CH:29]=[CH:28][C:27]([C:21]2[C:22]([CH3:26])=[CH:23][CH:24]=[CH:25][C:20]=2[CH3:19])=[CH:32][CH:31]=1)=[O:7])=[O:18])=[O:44]